EnhancerDB
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  3. TCF7L2[chr17:76381540-76386623]
Chromosome characteristics of TCF7L2[chr17:76381540-76386623]
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Enhancers possibly regulated by TCF7L2[chr17:76381540-76386623]
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Chrom Start End Enhancer ID Tissues that enhancer appears More
chr17 76375869 76387065 enh4624
Blood (T-cell) Esophagus Blood (OCI-LY7) Blood (GM12878) Placenta Thyroid Uterus Peripheral Blood (MM.1S) Blood (Karpas-422) Neural Stem Cells (H9) Thymus Heart
chr17 76382008 76383398 vista26206
VISTA
chr17 76384421 76384943 vista26207
VISTA
SNP sites on TCF7L2[chr17:76381540-76386623]
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Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr17 76381602 rs551773967 C A,T 5086277
chr17 76381650 rs554416730 G A 5086278
chr17 76381657 rs185264063 G C 5086279
chr17 76381677 rs556746546 T C 5086280
chr17 76381743 rs8070806 A C 5086281
chr17 76381760 rs560811506 C CT 5086282
chr17 76381783 rs545681142 G A,T 5086283
chr17 76381805 rs571836909 C CG 5086284
chr17 76381806 rs190849776 G A,T 5086285
chr17 76381870 rs530991095 GT G 5086286
chr17 76381997 rs549587801 C T 5086287
chr17 76382018 rs183398055 G A 5086288
chr17 76382079 rs4366775 C T 5086289
chr17 76382145 rs373952320 T C 5086290
chr17 76382179 rs62080360 C T 5086291
chr17 76382206 rs76129595 C A,G 5086292
chr17 76382215 rs370773356 T G 5086293
chr17 76382255 rs375700360 G A 5086294
chr17 76382260 rs376222105 G A,C 5086295
chr17 76382291 rs368530439 C G 5086296
chr17 76382296 rs56971055 A C 5086297
chr17 76382364 rs532224647 G A 5086298
chr17 76382400 rs371832844 A G 5086299
chr17 76382417 rs376439631 A G 5086300
chr17 76382433 rs368053984 C A 5086301
chr17 76382509 rs191954904 G C 5086302
chr17 76382542 rs182830619 C T 5086303
chr17 76382791 rs12948394 C T 5086304
chr17 76382950 rs12938284 C A 5086305
chr17 76383053 rs112325177 A G 5086306
chr17 76383062 rs60925600 G A 5086307
chr17 76383071 rs61550477 G A 5086308
chr17 76383089 rs62075736 G A 5086309
chr17 76383124 rs115913338 C T 5086310
chr17 76383229 rs554891531 C T 5086311
chr17 76383234 rs192144272 G A 5086312
chr17 76383313 rs113785037 G A 5086313
chr17 76383318 rs186931902 C T 5086314
chr17 76383319 rs62075738 A G 5086315
chr17 76383333 rs62075739 T C 5086316
chr17 76383372 rs111956193 A G 5086317
chr17 76383375 rs150521956 G C 5086318
chr17 76383444 rs372563335 G A,T 5086319
chr17 76383509 rs112055890 TAGCTGGG T 5086320
chr17 76383509 rs58487305 TAGCTGGG T 5086321
chr17 76383568 rs189854117 T C 5086322
chr17 76383607 rs59249646 T C 5086323
chr17 76383621 rs193166918 A C 5086324
chr17 76383637 rs184571736 C T 5086325
chr17 76383671 rs55938653 C T 5086326
chr17 76383679 rs34252361 CT C 5086327
chr17 76383712 rs573246069 G A 5086328
chr17 76383766 rs12450784 G A 5086329
chr17 76383807 rs55894414 G A 5086330
chr17 76383832 rs139328107 C T 5086331
chr17 76383969 rs530990986 G A 5086332
chr17 76384133 rs144079696 T C 5086333
chr17 76384220 rs62075741 G A 5086334
chr17 76384232 rs555881848 C T 5086335
chr17 76384254 rs569100911 G A 5086336
chr17 76384276 rs79584080 G A 5086337
chr17 76384278 rs62075742 G C 5086338
chr17 76384291 rs577821538 A G 5086339
chr17 76384315 rs62075743 T C 5086340
chr17 76384339 rs188255014 C T 5086341
chr17 76384417 rs78699298 A C,G 5086342
chr17 76384438 rs62075744 C T 5086343
chr17 76384482 rs151269639 GTTTC G 5086344
chr17 76384518 rs564810222 C T 5086345
chr17 76384533 rs73999305 A G 5086346
chr17 76384534 rs73999306 T C 5086347
chr17 76384587 rs199788641 T TA 5086348
chr17 76384587 rs535784596 T A 5086349
chr17 76384588 rs148962996 T A 5086350
chr17 76384627 rs375698898 A G 5086351
chr17 76384680 rs62075745 G A 5086352
chr17 76384743 rs74909528 G A 5086353
chr17 76384841 rs75313635 C T 5086354
chr17 76384897 rs138935218 A ACTGT 5086355
chr17 76384897 rs79124936 A ACTGT 5086356
chr17 76385021 rs8068516 C T 5086357
chr17 76385044 rs8069695 T C 5086358
chr17 76385067 rs398058922 TAAGTTGAAC T 5086359
chr17 76385067 rs55646759 TAAGTTGAAC T 5086360
chr17 76385159 rs551566067 G A,C 5086361
chr17 76385161 rs56117688 G T 5086362
chr17 76385200 rs143971337 A AT 5086363
chr17 76385207 rs533969963 G C 5086364
chr17 76385208 rs151048101 A G 5086365
chr17 76385263 rs555694882 C T 5086366
chr17 76385267 rs8068866 C T 5086367
chr17 76385310 rs8073753 T C 5086368
chr17 76385331 rs8072666 C A 5086369
chr17 76385381 rs8072820 C T 5086370
chr17 76385418 rs139310469 G A 5086371
chr17 76385492 rs143298395 T C 5086372
chr17 76385555 rs150463295 C T 5086373
chr17 76385582 rs190203072 A G 5086374
chr17 76385655 rs80131519 GCCTCCCAAAGTAC G 5086375
chr17 76385703 rs34954607 C CT,CTT 5086376
chr17 76385703 rs75371359 C CT 5086377
chr17 76385723 rs138269598 C A 5086378
chr17 76385825 rs192119437 G A 5086379
chr17 76385920 rs186680234 C T 5086380
chr17 76385957 rs563156657 A G 5086381
chr17 76385961 rs576408844 T C 5086382
chr17 76386037 rs12452576 A C 5086383
chr17 76386067 rs191489872 A G 5086384
chr17 76386149 rs183256169 G A,C 5086385
chr17 76386229 rs117742687 C G 5086386
chr17 76386274 rs2090205 C A 5086387
chr17 76386318 rs368053744 C A,G 5086388
chr17 76386335 rs8077859 C T 5086389
chr17 76386406 rs7222619 T C,G 5086390
chr17 76386412 rs7503405 A G 5086391
chr17 76386416 rs183375876 A G 5086392
chr17 76386449 rs193151588 C T 5086393
chr17 76386578 rs7221930 G T 5086394
chr17 76386597 rs138529392 C G,T 5086395
Genes possibly regulated by TCF7L2[chr17:76381540-76386623]
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Details of Genes
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand Gene Name Ensembl ID TSS TSI of Normal tissues TSI of Cancer tissues Distance to TFBS id More
Expression level of Genes
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No results
miRNAs possibly regulated by TCF7L2[chr17:76381540-76386623]
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Details of miRNAs
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End strand miRNA Name miRBase ID TSS TSI of Normal tissues TSI of Cancer tissues Distance to TFBS id More
Expression level of miRNAs
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No results